Molecular structure of 2-Hydroxybenzophenone, CAS Number: 117-99-7
2-Hydroxybenzophenone (CAS 117-99-7)
Alternate Names:
2-Benzoylphenol
CAS Number:
117-99-7
Molecular Weight:
198.22
Molecular Formula:
HOC6H4COC6H5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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2-Hydroxybenzophenone has found utility in the realm of organic chemistry as a valuable building block for synthesizing diverse organic compounds. Its versatile nature enables it to serve as a reactant in numerous chemical reactions. Moreover, scientists have investigated the potential of 2-Hydroxybenzophenone as useful in polymer synthesis and the creation of other materials.
2-Hydroxybenzophenone (CAS 117-99-7) References
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- Systematic study of the luminescent europium-based nonanuclear clusters with modified 2-hydroxybenzophenone ligands. | Zhang, B., et al. 2013. Inorg Chem. 52: 13332-40. PMID: 24224576
- A reevaluation of the photolytic properties of 2-hydroxybenzophenone-based UV sunscreens: are chemical sunscreens inoffensive? | Ignasiak, MT., et al. 2015. Chemphyschem. 16: 628-33. PMID: 25581220
- Physicochemical characterization of 2-hydroxybenzophenone with β-cyclodextrin in solution and solid state. | Sancho, MI., et al. 2015. J Phys Chem B. 119: 5918-25. PMID: 25893377
- Regioselective construction of diverse and multifunctionalized 2-hydroxybenzophenones for sun protection by indium(iii)-catalyzed benzannulation. | Cai, H., et al. 2016. Chem Commun (Camb). 52: 7661-4. PMID: 27126271
- 2-Hydroxybenzophenone as a Chemical Auxiliary for the Activation of Ketiminoesters for Highly Enantioselective Addition to Nitroalkenes under Bifunctional Catalysis. | Guerrero-Corella, A., et al. 2018. Angew Chem Int Ed Engl. 57: 5350-5354. PMID: 29493860
- Intramolecular hydrogen-bond activation for the addition of nucleophilic imines: 2-hydroxybenzophenone as a chemical auxiliary. | Choubane, H., et al. 2018. Chem Commun (Camb). 54: 3399-3402. PMID: 29557452
- Hydrogen-Bonding-Assisted Ketimine Formation of Benzophenone Derivatives. | Seo, MS., et al. 2018. J Org Chem. 83: 14300-14306. PMID: 30398053
- Transition-metal-free cascade benzannulations for synthesizing 2-hydroxybenzophenones. | He, XW., et al. 2020. Org Biomol Chem. 18: 9039-9043. PMID: 33141141
- Simultaneous trace analysis of 10 benzophenone-type ultraviolet filters in fish through liquid chromatography-tandem mass spectrometry. | Huang, YF., et al. 2021. Environ Pollut. 286: 117306. PMID: 33991738
- 2-Hydroxybenzophenone Derivatives: ESIPT Fluorophores Based on Switchable Intramolecular Hydrogen Bonds and Excitation Energy-Dependent Emission. | Wang, H., et al. 2021. Front Chem. 9: 766179. PMID: 34738006
- Cumulative Dietary Risk Assessment of Benzophenone-Type Photoinitiators from Packaged Foodstuffs. | Chen, ML., et al. 2022. Foods. 11: PMID: 35053884
- Identification of Benzophenone Analogs in Rice Cereal through Fast Pesticide Extraction and Ultrahigh-Performance Liquid Chromatography-Tandem Mass Spectrometry. | Liu, XR., et al. 2022. Foods. 11: PMID: 35206047
- Rapid determination of benzophenone derivatives in cereals using FaPEx coupled with ultra-high-performance liquid chromatography-tandem mass spectrometry. | Huang, YF., et al. 2021. J Food Drug Anal. 29: 287-302. PMID: 35696205
- The binding mechanism of benzophenone-type UV filters and human serum albumin: The role of site, number, and type of functional group substitutions. | Ma, J., et al. 2023. Environ Pollut. 324: 121342. PMID: 36828352
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Hydroxybenzophenone, 5 g | sc-223444 | 5 g | $51.00 | |||
2-Hydroxybenzophenone, 25 g | sc-223444A | 25 g | $149.00 |